Role of the alternative splice variant of NCC in blood pressure control

av Wardak, Hila, Tutakhel, Omar A.Z., Van Der Wijst, Jenny
I publikationen Channels (Austin) (2018)

High‐resolution structures of transient receptor potential vanilloid channels: Unveiling a functionally diverse group of ion channels

av van Goor, Mark K., de Jager, Leanne, Cheng, Yifan, van der Wijst, Jenny
I publikationen Protein Sci (2020)

Renal sodium and magnesium reabsorption are not coupled in a mouse model of Gordon syndrome

av van Megen, Wouter H., Grimm, Paul R., Welling, Paul A., van der Wijst, Jenny
I publikationen Physiol Rep (2018)

Regulation of Two Renal Chloride Transporters, AE1 and Pendrin, by Electrolytes and Aldosterone

av Mohebbi, Nilufar, Perna, Angelica, van der Wijst, Jenny, Becker, Helen M., Capasso, Giovambattista, Wagner, Carsten A.
Publicerad 2013

Interspecies differences in PTH-mediated PKA phosphorylation of the epithelial calcium channel TRPV5

av van Goor, Mark K, Verkaart, Sjoerd, van Dam, Teunis J, Huynen, Martijn A, van der Wijst, Jenny
I publikationen Pflugers Arch (2017)

Structural insight into TRPV5 channel function and modulation

av Dang, Shangyu, van Goor, Mark K., Asarnow, Daniel, Wang, YongQiang, Julius, David, Cheng, Yifan, van der Wijst, Jenny
I publikationen Proc Natl Acad Sci U S A (2019)

Regulation of the Epithelial Mg(2+) Channel TRPM6 by Estrogen and the Associated Repressor Protein of Estrogen Receptor Activity (REA)

av Cao, Gang, van der Wijst, Jenny, van der Kemp, AnneMiete, van Zeeland, Femke, Bindels, René J., Hoenderop, Joost G.
Publicerad 2009

Functional Analysis of the Kv1.1 N255D Mutation Associated with Autosomal Dominant Hypomagnesemia

av van der Wijst, Jenny, Glaudemans, Bob, Venselaar, Hanka, Nair, Anil V., Forst, Anna-Lena, Hoenderop, Joost G. J., Bindels, René J. M.
Publicerad 2010

New TRPM6 missense mutations linked to hypomagnesemia with secondary hypocalcemia

av Lainez, Sergio, Schlingmann, Karl Peter, van der Wijst, Jenny, Dworniczak, Bernd, van Zeeland, Femke, Konrad, Martin, Bindels, René J, Hoenderop, Joost G
Publicerad 2014

A Gate Hinge Controls the Epithelial Calcium Channel TRPV5

av van der Wijst, Jenny, Leunissen, Elizabeth H., Blanchard, Maxime G., Venselaar, Hanka, Verkaart, Sjoerd, Paulsen, Candice E., Bindels, René J., Hoenderop, Joost G.
I publikationen Sci Rep (2017)

Methionine Sulfoxide Reductase B1 (MsrB1) Recovers TRPM6 Channel Activity during Oxidative Stress

av Cao, Gang, Lee, Kyu pil, van der Wijst, Jenny, de Graaf, Mark, van der Kemp, AnneMiete, Bindels, René J. M., Hoenderop, Joost G. J.
Publicerad 2010

Effects of the EGFR Inhibitor Erlotinib on Magnesium Handling

av Dimke, Henrik, van der Wijst, Jenny, Alexander, Todd R., Meijer, Inez M.J., Mulder, Gemma M., van Goor, Harry, Tejpar, Sabine, Hoenderop, Joost G., Bindels, René J.
Publicerad 2010

A de novo KCNA1 Mutation in a Patient with Tetany and Hypomagnesemia

av van der Wijst, Jenny, Konrad, Martin, Verkaart, Sjoerd A.J., Tkaczyk, Marcin, Latta, Femke, Altmüller, Janine, Thiele, Holger, Beck, Bodo, Schlingmann, Karl Peter, de Baaij, Jeroen H.F.
I publikationen Nephron Clin Pract (2018)

A missense mutation in the Kv1.1 voltage-gated potassium channel–encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia

av Glaudemans, Bob, van der Wijst, Jenny, Scola, Rosana H., Lorenzoni, Paulo J., Heister, Angelien, van der Kemp, AnneMiete W., Knoers, Nine V., Hoenderop, Joost G., Bindels, René J.
Publicerad 2009

Renal Handling of Circulating and Renal-Synthesized Hepcidin and Its Protective Effects against Hemoglobin–Mediated Kidney Injury

av van Swelm, Rachel P.L., Wetzels, Jack F.M., Verweij, Vivienne G.M., Laarakkers, Coby M.M., Pertijs, Jeanne C.L.M., van der Wijst, Jenny, Thévenod, Frank, Masereeuw, Rosalinde, Swinkels, Dorine W.
I publikationen J Am Soc Nephrol (2016)

Impaired basolateral sorting of pro-EGF causes isolated recessive renal hypomagnesemia

av Groenestege, Wouter M. Tiel, Thébault, Stéphanie, van der Wijst, Jenny, van den Berg, Dennis, Janssen, Rob, Tejpar, Sabine, van den Heuvel, Lambertus P., van Cutsem, Eric, Hoenderop, Joost G., Knoers, Nine V., Bindels, René J.
Publicerad 2007

Targeted Next-Generation Sequencing of a 12.5 Mb Homozygous Region Reveals ANO10 Mutations in Patients with Autosomal-Recessive Cerebellar Ataxia

av Vermeer, Sascha, Hoischen, Alexander, Meijer, Rowdy P.P., Gilissen, Christian, Neveling, Kornelia, Wieskamp, Nienke, de Brouwer, Arjan, Koenig, Michel, Anheim, Mathieu, Assoum, Mirna, Drouot, Nathalie, Todorovic, Slobodanka, Milic-Rasic, Vedrana, Lochmüller, Hanns, Stevanin, Giovanni, Goizet, Cyril, David, Albert, Durr, Alexandra, Brice, Alexis, Kremer, Berry, van de Warrenburg, Bart P.C., Schijvenaars, Mascha M.V.A.P., Heister, Angelien, Kwint, Michael, Arts, Peer, van der Wijst, Jenny, Veltman, Joris, Kamsteeg, Erik-Jan, Scheffer, Hans, Knoers, Nine
Publicerad 2010